Canonical Allele Identifier: CA445404236

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90755176-C-A
• MyVariant Identifiers: chr5:g.90050993C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755176C>A , CM000667.2:g.90755176C>A	GRCh38
NC_000005.9:g.90050993C>A , CM000667.1:g.90050993C>A	GRCh37
NC_000005.8:g.90086749C>A	NCBI36
NG_007083.1:g.201377C>A
NG_007083.2:g.230833C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11571C>A MANE Select	ENSP00000384582.2:p.Ser3857=
ENST00000425867.3:c.702C>A	ENSP00000392618.3:p.Ser234=
ENST00000639431.1:c.265+78967C>A	ENSP00000491057.1:n.265+78967C>A
ENST00000640374.1:n.4715C>A
ENST00000640464.1:n.1990C>A
ENST00000405460.6:c.11571C>A	ENSP00000384582.2:p.Ser3857=
ENST00000509621.1:c.4268C>A
NM_032119.3:c.11571C>A	NP_115495.3:p.Ser3857=
NR_003149.1:n.11584C>A
XM_011543675.1:c.11568C>A	XP_011541977.1:p.Ser3856=
XM_011543676.1:c.11490C>A	XP_011541978.1:p.Ser3830=
XM_011543677.1:c.8874C>A	XP_011541979.1:p.Ser2958=
XM_011543678.1:c.11571C>A	XP_011541980.1:p.Ser3857=
NM_032119.4:c.11571C>A MANE Select	NP_115495.3:p.Ser3857=
XM_017009963.2:c.11592C>A	XP_016865452.1:p.Ser3864=
XM_017009964.2:c.11589C>A	XP_016865453.1:p.Ser3863=
XM_017009965.1:c.11589C>A	XP_016865454.1:p.Ser3863=
XM_017009966.2:c.11511C>A	XP_016865455.1:p.Ser3837=
XM_017009967.1:c.11496C>A	XP_016865456.1:p.Ser3832=
XM_017009968.2:c.11592C>A	XP_016865457.1:p.Ser3864=
XM_017009969.2:c.11592C>A	XP_016865458.1:p.Ser3864=
XM_017009970.2:c.11592C>A	XP_016865459.1:p.Ser3864=
XM_017009971.2:c.11592C>A	XP_016865460.1:p.Ser3864=
XM_017009972.1:c.4710C>A	XP_016865461.1:p.Ser1570=
XM_017009973.1:c.4689C>A	XP_016865462.1:p.Ser1563=
NR_003149.2:n.11587C>A